Common mutations in ALK2/ACVR1, a multi-faceted receptor, have roles in distinct pediatric musculoskeletal and neural orphan disorders.
about
Activin receptor-like kinases: a diverse family playing an important role in cancerNovel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva.Fibrodysplasia ossificans progressiva: Basic understanding and experimental models.Bone Morphogenetic Proteins.Acquired and congenital forms of heterotopic ossification: new pathogenic insights and therapeutic opportunities.
P2860
Common mutations in ALK2/ACVR1, a multi-faceted receptor, have roles in distinct pediatric musculoskeletal and neural orphan disorders.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Common mutations in ALK2/ACVR1 ...... l and neural orphan disorders.
@ast
Common mutations in ALK2/ACVR1 ...... l and neural orphan disorders.
@en
type
label
Common mutations in ALK2/ACVR1 ...... l and neural orphan disorders.
@ast
Common mutations in ALK2/ACVR1 ...... l and neural orphan disorders.
@en
prefLabel
Common mutations in ALK2/ACVR1 ...... l and neural orphan disorders.
@ast
Common mutations in ALK2/ACVR1 ...... l and neural orphan disorders.
@en
P2860
P1476
Common mutations in ALK2/ACVR1 ...... l and neural orphan disorders.
@en
P2093
Eileen M Shore
Maurizio Pacifici
P2860
P304
P356
10.1016/J.CYTOGFR.2015.12.007
P577
2015-12-28T00:00:00Z